Evidence map›Paper›PMID 37612099›Full record

ArticleBMJ open respiratory research2023

Phenotyping asthma with airflow obstruction in middle-aged and older adults: a CADSET clinical research collaboration.

Xander Bertels, Ahmed Edris, Judith Garcia-Aymerich, Rosa Faner, Howraman Meteran, Torben Sigsgaard, Peter Alter, Claus Vogelmeier, Nuria Olvera, Nazanin Zounemat Kermani and 12 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open respiratory research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 8 institutions in 8 countries.

Xander BertelsDepartment of Bioanalysis, Ghent University, Gent, Belgium.ORCID 0000-0002-4815-9067
Ahmed EdrisDepartment of Bioanalysis, Ghent University, Gent, Belgium.ORCID 0000-0002-4049-5402
Judith Garcia-AymerichNon-Communicable Diseases and Environment Programme, ISGlobal, Barcelona, Spain.ORCID 0000-0002-7097-4586
Rosa FanerCentro Investigaciones Biomédicas en Red (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Howraman MeteranDepartment of Respiratory Medicine, Copenhagen University Hospital-Amager and Hvidovre, Kobenhagen, Denmark.
Torben SigsgaardEnvironment, Occupation and Health, Danish Ramazzini Centre, Department of Public Health, Aarhus University, Aarhus, Denmark.
Peter AlterDepartment of Medicine, Pulmonary and Critical Care Medicine, Philipps University of Marburg, Marburg, Germany.
Claus VogelmeierDepartment of Medicine, Pulmonary and Critical Care Medicine, Philipps University of Marburg, Marburg, Germany.
Nuria OlveraCentro Investigaciones Biomédicas en Red (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Nazanin Zounemat KermaniNational Heart and Lung Institute & Data Science Institute, Imperial College London, London, UK.
Alvar AgustiCentro Investigaciones Biomédicas en Red (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Gavin C DonaldsonNational Heart and Lung Institute & Data Science Institute, Imperial College London, London, UK.ORCID 0000-0002-5538-4190
Jadwiga A WedzichaNational Heart and Lung Institute & Data Science Institute, Imperial College London, London, UK.
Guy G BrusselleDepartment of Epidemiology, Erasmus MC, Rotterdam, The Netherlands.
Helena BackmanDepartment of Public Health and Clinical Medicine, Umeå University, Umea, Sweden.
Eva RönmarkDepartment of Public Health and Clinical Medicine, Umeå University, Umea, Sweden.
Anne LindbergDepartment of Public Health and Clinical Medicine, Umeå University, Umea, Sweden.ORCID 0000-0002-3292-7471
Judith M VonkDepartment of Epidemiology, University Medical Centre Groningen, Groningen, The Netherlands.
Kian Fan ChungNational Heart and Lung Institute & Data Science Institute, Imperial College London, London, UK.
Ian M AdcockNational Heart and Lung Institute & Data Science Institute, Imperial College London, London, UK.ORCID 0000-0003-2101-8843
Maarten van den BergeGroningen Research Institute for Asthma and COPD (GRIAC), University Medical Centre Groningen, Groningen, The Netherlands.
Lies LahousseDepartment of Bioanalysis, Ghent University, Gent, Belgium lies.lahousse@ugent.be.ORCID 0000-0002-3494-4363
Imperial College London · GBInstituto de Salud Carlos III · ESErasmus MC · NLUmeå University · SEAarhus University · DKPhilipps University of Marburg · DEUniversity Medical Center Groningen · NLGhent University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence and clinical profile of asthma with airflow obstruction (AO) remain uncertain. We aimed to phenotype AO in population- and clinic-based cohorts.

methodsThis cross-sectional multicohort study included adults ≥50 years from nine CADSET cohorts with spirometry data (N=69 789). AO was defined as ever diagnosed asthma with pre-BD or post-BD FEV

resultsThe prevalence of AO was 2.1% (95% CI 2.0% to 2.2%) in population-based, 21.1% (95% CI 18.6% to 23.8%) in asthma-based and 16.9% (95% CI 15.8% to 17.9%) in COPD-based cohorts. AO patients had more often clinically relevant dyspnoea (modified Medical Research Council score ≥2) than asthma-only (+14.4 and +14.7 percentage points) and COPD-only (+24.0 and +5.0 percentage points) in population-based and clinic-based cohorts, respectively. AO patients had more often elevated blood eosinophil counts (>300 cells/µL), although only significant in population-based cohorts. Compared with asthma-only, AO patients were more often men, current smokers, with a lower BMI, had less often obesity and had more often chronic bronchitis. Compared with COPD-only, AO patients were younger, less often current smokers and had less pack-years. In the general population, AO patients had a higher risk of coronary artery disease than asthma-only and COPD-only (OR=2.09 (95% CI 1.26 to 3.47) and OR=1.89 (95% CI 1.10 to 3.24), respectively) and of depression (OR=1.41 (95% CI 1.19 to 1.67)), osteoporosis (OR=2.30 (95% CI 1.43 to 3.72)) and gastro-oesophageal reflux disease (OR=1.68 (95% CI 1.06 to 2.68)) than COPD-only, independent of age, sex, smoking status and BMI.

conclusionsAO is a relatively prevalent respiratory phenotype associated with more dyspnoea and a higher risk of coronary artery disease and elevated blood eosinophil counts in the general population compared with both asthma-only and COPD-only.

Indexed as

AsthmaCoronary Artery DiseasePulmonary Disease, Chronic ObstructiveCross-Sectional StudiesDyspneaHumansMaleAsthmaAsthma EpidemiologyClinical EpidemiologyCOPD epidemiologyPulmonary Disease, Chronic Obstructive

Identifiers

PMID37612099
PMCPMC10450061
OpenAlexW4386101962

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.